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T Liehr

Showing results (151-160 of 192) with videos related to

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Cytogenetics and Cell Genetics|February 15, 2001
Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndromeA Dufke, J Seidel, M Schöning, et al.
Human Reproduction (Oxford, England)|February 4, 2005
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failureM Oliver-Bonet, J Benet, F Sun, et al.
Clinical Genetics|March 19, 2010
An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patientB Auber, P Burfeind, C Thiels, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangementsT Liehr, N Kosayakova, J Schröder, et al.
Cytogenetic and Genome Research|November 13, 2013
Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysisS S Bhatt, M Manvelyan, K Moradkhani, et al.
Bulletin of Experimental Biology and Medicine|November 21, 2007
Chromosome variability of human multipotent mesenchymal stromal cellsN P Bochkov, E S Voronina, N V Kosyakova, et al.
Cytogenetic and Genome Research|September 5, 2009
Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlationJ B Melo, E Matoso, A Polityko, et al.
International Journal of Molecular Medicine|January 22, 2008
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell levelA Weise, M Gross, K Mrasek, et al.
Prenatal Diagnosis|May 22, 2001
Pitfalls of rapid prenatal diagnosis using the interphase nucleusT Liehr, V Beensen, R Hauschild, et al.
Cytogenetic and Genome Research|February 18, 2006
Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanismsC Rudolph, T Liehr, D Steinemann, et al.
Pageof 20

Showing results (151-160 of 192) with videos related to

Sort By:
Pageof 20
Cytogenetics and Cell Genetics|February 15, 2001
Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndromeA Dufke, J Seidel, M Schöning, et al.
Human Reproduction (Oxford, England)|February 4, 2005
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failureM Oliver-Bonet, J Benet, F Sun, et al.
Clinical Genetics|March 19, 2010
An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patientB Auber, P Burfeind, C Thiels, et al.
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangementsT Liehr, N Kosayakova, J Schröder, et al.
Cytogenetic and Genome Research|November 13, 2013
Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysisS S Bhatt, M Manvelyan, K Moradkhani, et al.
Bulletin of Experimental Biology and Medicine|November 21, 2007
Chromosome variability of human multipotent mesenchymal stromal cellsN P Bochkov, E S Voronina, N V Kosyakova, et al.
Cytogenetic and Genome Research|September 5, 2009
Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlationJ B Melo, E Matoso, A Polityko, et al.
International Journal of Molecular Medicine|January 22, 2008
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell levelA Weise, M Gross, K Mrasek, et al.
Prenatal Diagnosis|May 22, 2001
Pitfalls of rapid prenatal diagnosis using the interphase nucleusT Liehr, V Beensen, R Hauschild, et al.
Cytogenetic and Genome Research|February 18, 2006
Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanismsC Rudolph, T Liehr, D Steinemann, et al.
Pageof 20